Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.4862810G>A | CA438366036 | MSX1 | c.579G>A (p.Gln193=) n.291G>A | |
4 | g.4862810G>C | CA356138402 | MSX1 | c.579G>C (p.Gln193His) n.291G>C | dbSNP gnomAD v2 gnomAD v4 |
4 | g.4862810G= | CA1435013662 | MSX1 | c.579G= (p.Gln193=) n.291G= | |
4 | g.4862810G>T | CA356138403 | MSX1 | c.579G>T (p.Gln193His) n.291G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.4862811A>C | CA356138404 | MSX1 | c.580A>C (p.Lys194Gln) n.292A>C | |
4 | g.4862811A>G | CA356138405 | MSX1 | c.580A>G (p.Lys194Glu) n.292A>G | |
4 | g.4862811A>T | CA356138406 | MSX1 | c.580A>T (p.Lys194Ter) n.292A>T | |
4 | g.4862812A= | CA1435013663 | MSX1 | c.581A= (p.Lys194=) n.293A= | |
4 | g.4862812A>C | CA356138407 | MSX1 | c.581A>C (p.Lys194Thr) n.293A>C | |
4 | g.4862812A>G | CA2833078 | MSX1 | c.581A>G (p.Lys194Arg) n.293A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.4862812A>T | CA356138408 | MSX1 | c.581A>T (p.Lys194Met) n.293A>T | |
4 | g.4862813G>A | CA2833079 | MSX1 | c.582G>A (p.Lys194=) n.294G>A | dbSNP ExAC gnomAD v2 |
4 | g.4862813G>C | CA356138409 | MSX1 | c.582G>C (p.Lys194Asn) n.294G>C | |
4 | g.4862813G= | CA1435013664 | MSX1 | c.582G= (p.Lys194=) n.294G= | |
4 | g.4862813G>T | CA356138410 | MSX1 | c.582G>T (p.Lys194Asn) n.294G>T | gnomAD v4 |
4 | g.4862814C>A | CA356138412 | MSX1 | c.583C>A (p.Gln195Lys) n.295C>A | gnomAD v4 COSMIC |
4 | g.4862814C>G | CA356138413 | MSX1 | c.583C>G (p.Gln195Glu) n.295C>G | |
4 | g.4862814C>T | CA356138411 | MSX1 | c.583C>T (p.Gln195Ter) n.295C>T | |
4 | g.4862815A>C | CA356138414 | MSX1 | c.584A>C (p.Gln195Pro) n.296A>C | gnomAD v4 |
4 | g.4862815A>G | CA356138415 | MSX1 | c.584A>G (p.Gln195Arg) n.296A>G | |
4 | g.4862815A>T | CA356138416 | MSX1 | c.584A>T (p.Gln195Leu) n.296A>T | |
4 | g.4862816G>A | CA438366040 | MSX1 | c.585G>A (p.Gln195=) n.297G>A | |
4 | g.4862816G>C | CA356138417 | MSX1 | c.585G>C (p.Gln195His) n.297G>C | |
4 | g.4862816G>T | CA356138418 | MSX1 | c.585G>T (p.Gln195His) n.297G>T | |
4 | g.4862817T>A | CA356138419 | MSX1 | c.586T>A (p.Tyr196Asn) n.298T>A | |
4 | g.4862817T>C | CA356138420 | MSX1 | c.586T>C (p.Tyr196His) n.298T>C | |
4 | g.4862817T>G | CA356138421 | MSX1 | c.586T>G (p.Tyr196Asp) n.298T>G | |
4 | g.4862818A>C | CA356138422 | MSX1 | c.587A>C (p.Tyr196Ser) n.299A>C | |
4 | g.4862818A>G | CA356138423 | MSX1 | c.587A>G (p.Tyr196Cys) n.299A>G | |
4 | g.4862818A>T | CA356138424 | MSX1 | c.587A>T (p.Tyr196Phe) n.299A>T | |
4 | g.4862819C>A | CA356138425 | MSX1 | c.588C>A (p.Tyr196Ter) n.300C>A | |
4 | g.4862819C= | CA1435013665 | MSX1 | c.588C= (p.Tyr196=) n.300C= | |
4 | g.4862819C>G | CA356138426 | MSX1 | c.588C>G (p.Tyr196Ter) n.300C>G | |
4 | g.4862819C>T | CA438366044 | MSX1 | c.588C>T (p.Tyr196=) n.300C>T | dbSNP gnomAD v2 gnomAD v4 |
4 | g.4862821_4862825dup | CA2586973673 | MSX1 | c.590_594dup (p.Ile199CysfsTer20) n.302_306dup | |
4 | g.4862820C>A | CA356138427 | MSX1 | c.589C>A (p.Leu197Met) n.301C>A | |
4 | g.4862820C>G | CA356138428 | MSX1 | c.589C>G (p.Leu197Val) n.301C>G | |
4 | g.4862820C>T | CA438366045 | MSX1 | c.589C>T (p.Leu197=) n.301C>T | |
4 | g.4862821T>A | CA356138429 | MSX1 | c.590T>A (p.Leu197Gln) n.302T>A | |
4 | g.4862821T>C | CA356138430 | MSX1 | c.590T>C (p.Leu197Pro) n.302T>C | |
4 | g.4862821T>G | CA356138431 | MSX1 | c.590T>G (p.Leu197Arg) n.302T>G | |
4 | g.4862822G>A | CA438366047 | MSX1 | c.591G>A (p.Leu197=) n.303G>A | |
4 | g.4862822G>C | CA438366049 | MSX1 | c.591G>C (p.Leu197=) n.303G>C | |
4 | g.4862822G>T | CA438366051 | MSX1 | c.591G>T (p.Leu197=) n.303G>T | |
4 | g.4862823T>A | CA356138432 | MSX1 | c.592T>A (p.Ser198Thr) n.304T>A | |
4 | g.4862823T>C | CA356138433 | MSX1 | c.592T>C (p.Ser198Pro) n.304T>C | |
4 | g.4862823T>G | CA356138434 | MSX1 | c.592T>G (p.Ser198Ala) n.304T>G | |
4 | g.4862824C>A | CA356138435 | MSX1 | c.593C>A (p.Ser198Tyr) n.305C>A | |
4 | g.4862824C>G | CA356138436 | MSX1 | c.593C>G (p.Ser198Cys) n.305C>G | |
4 | g.4862824C>T | CA356138437 | MSX1 | c.593C>T (p.Ser198Phe) n.305C>T |